Distribution of cionin, a cholecystokinin/gastrin family peptide, and its receptor in the central nervous system of Ciona intestinalis type A

The cholecystokinin (CCK)/gastrin family peptides are involved in regulation of feeding and digestion in vertebrates. In the ascidian Ciona intestinalis type A (Ciona robusta), cionin, a CCK/gastrin family peptide, has been identified. Cionin is expressed exclusively in the central nervous system (CNS). In contrast, cionin receptor expression has been detected in the CNS, digestive tract, and ovary. Although cionin has been reported to be involved in ovulation, its physiological function in the CNS remains to be investigated. To elucidate its neural function, in the present study, we analyzed the expression of cionin and cionin receptors in the CNS. Cionin was expressed mainly in neurons residing in the anterior region of the cerebral ganglion. In contrast, the gene expressin of the cionin receptor gene CioR1, was detected in the middle part of the cerebral ganglion and showed a similar expression pattern to that of VACHT, a cholinergic neuron marker gene. Moreover, CioR1 was found to be expressed in cholinergic neurons. Consequently, these results suggest that cionin interacts with cholinergic neurons as a neurotransmitter or neuromodulator via CioR1. This study provides insights into a biological role of a CCK/gastrin family peptide in the CNS of ascidians.

. The previous study showed that cionin is expressed in the cerebral ganglion.However, the precise localization of cionin in the cerebral ganglion remains to be elucidated.
In the present study, we evaluated the precise distribution of cionin peptides in the neural complex by immunohistochemical analysis of serial sections of the neural complex using anti-cionin antibody.In sections that included the anterior region, cionin-immunopositive cell bodies were accumulated in the anterior part of the cerebral ganglion (Figs.1A,B).Moreover, cionin-positive fibers were observed in the middle and posterior parts of the cerebral ganglion (Figs.1B-D).The distribution of cionin-immunopositive neurites was detected mainly in the inner layer of the cerebral ganglion, whereas a part of cionin immunopositive nerve fivers projected toward the outer layer of the cerebral ganglion (Figs.1B,C).These results revealed that the cioninergic neurons possess a cell body in the anterior region, and their fibers are distributed in the middle and posterior regions of the cerebral ganglion.

Localization of CioR1 and 2 mRNA in juvenile and adult neural complex
In our previous study, CioR1 mRNA was shown to be expressed in the neural complex, ovary, stomach, intestine, oral siphon, and atrial siphon, and CioR2 mRNA was detected in the neural complex, endostyle, ovary, oral siphon, and atrial siphon 18 .
To evaluate the localization of CioR1 and 2 mRNA in the neural complex, we performed whole mount in situ hybridization (WISH) on juvenile Ciona.CioR1 mRNA was predominantly localized to the cerebral ganglion (Figs.2A,B).In addition, WISH of the adult neural complex demonstrated that the CioR1 mRNA was detected in the outer layer of the cerebral ganglion, which mainly consists of the cell bodies of neurons (Figs.2D,E).On the other hand, the signal of CioR2 mRNA was detected in a limited number of cerebral ganglion cells and the neural gland (Figs.2F,G).This localization pattern was also detected in the adult neural complex (Figs.2H,I).These findings clarified that CioR1 and 2 are expressed dominantly in the cerebral ganglion and neural gland, respectively.

Evaluation of the co-expression of cionin, CioR1, and VACHT
To confirm the cionin and CioR1-expressing regions, we performed WISH of the adult neural complex.Cionin mRNA expression was observed in the anterior region of the cerebral ganglion (Figs.3A,B).The CioR1 mRNA was expressed in the central region of the cerebral ganglion (Figs.3C,D).The spatial expression pattern of CioR1 mRNA was similar to that of VACHT mRNA, a marker of cholinergic neurons (Figs.3E,F).
To clarify the co-expression of cionin and CioR1 mRNA with VACHT mRNA, we conducted double in situ hybridization of the neural complex.Double in situ hybridization using cionin and VACHT probes indicated that cionin-positive signals did not overlap with VACHT signals in the cerebral ganglion as the result of WISH analysis (Figs. 4A-D).Next, we performed double in situ hybridization analysis using CioR1 and VACHT probes.In the middle of the cerebral ganglion, cells co-expressing CioR1 and VACHT were detected, since the CioR1 mRNA was detected in VACHT-positive cell population (Figs.4E-I).These results demonstrated that CioR1 is expressed in several cholinergic neurons.

Discussion
Ascidians are the extant animal group closest to vertebrates 21 .In addition to its phylogenetic position, genome information of some ascidians has been available in the public database 22,23 .In particular, C. intestinalis type A is a useful model for ascidians.Furthermore, various developmental engineering technologies, such as transgenic and genome-editing techniques, have been established in Ciona 22,24 .Therefore, Ciona is considered to be a primitive chordate model in both evolutionary and developmental biology.Recently, studies on the evolution of the nervous and endocrine systems have made progress in Ciona.Peptides and their receptors, which are prerequisites for the regulation of the nervous and endocrine systems, have been identified [25][26][27] .Furthermore, multiple Ciona-specific peptide-receptor pairs have thus far been elucidated 28 .These findings indicate that Ciona also has been regarded as a model animal to study the evolution of the endocrine and nervous systems in chordates.We have investigated Ciona CCK/gastrin family peptide, cionin.Since cionin has vertebrate-type CCK/ gastrin family peptide characteristics in its primary structure, the investigation of the neural function of cionin will contribute to clarifying the origin and diversification of CCK/gastrin family peptides in vertebrates.Our previous study uncovered the tissue distribution of cionin, CioRs mRNA, and the ligand-receptor relationship between cionin and CioRs 18 .Recently, the peripheral action of cionin has been elucidated.Osugi et al. showed that cionin elicits ovulation via CioR2 expressed in the Ciona ovarian follicle cells 29 .However, a biological function of cionin in the central nervous system remains unsolved.Therefore, we analyzed the localization of cionin and CioRs in the central nervous system in detail.
Cionin-immunopositive neurons and nerve fibers were detected in the anterior and middle/posterior regions of the cerebral ganglion, respectively, suggesting that these fibers run from the cell body in the anterior part of the cerebral ganglion.WISH analysis of CioRs revealed that CioR1 mRNA was localized throughout the entire cerebral ganglion of juvenile and adult neural complex (Figs.2A-D).In contrast, transcripts of CioR2 were detected mainly in the neural gland of juvenile and adult neural complex (Figs.2E-G).Since the expression of CioR2 was non-neuronal, CioR2 was excluded from the subject of further research.The expression of cionin mRNA in the neural complex was compared with that of CioR1 mRNA by WISH (Fig. 3).Cionin mRNA expression was restricted to the anterior part of the cerebral ganglion in accordance with the result of the immunohistochemistry of the serial section of the neural complex (Figs.1B, 3A,B).CioR1 mRNA localization was observed in the central part of the cerebral ganglion.The spatial expression pattern of CioR1 mRNA was similar to that of the cholinergic neuron marker, VACHT mRNA (Figs. 3C-F).Double in situ hybridization demonstrated that several the cholinergic neuronal cell bodies expressed CioR1 in the central region (Fig. 4).Additionally, cionin-immunopositive fibers were detected in the vicinity of the outer layer of the middle part of the cerebral ganglion, where CioR1-positive cholinergic neurons were observed.In mammals, CCK is associated with cholinergic neurons or acetylcholine-expressing cells as a transmitter or modulator 30,31 .For instance, CCK-8 modulates the release of acetylcholine in the rat striatum 30 .These findings indicate the possibility that cioninergic neurons regulate the function of cholinergic neurons via CioR1.Further studies on the direct interaction between CioR1-expressing cholinergic and cioninergic neurons are necessary.Cholinergic neuron distribution has been reported using the VACHT promoter-driven Kaede marker transgenic juvenile Ciona 32 and have been detected throughout the juvenile cerebral ganglion 32 .These findings seem to be in contrast with the present WISH analysis (Fig. 4).However, the major expression area of the VACHT promoter-driven Kaede was observed in the central region, similar to the expression area of VACHT detected by WISH (Fig. 4).It has been reported that acetylcholine released from the cholinergic nerve terminals is involved in the contraction of ascidian body muscle 33,34 .Moreover, expression analysis using the Ciona marker transgenic line driven by the VACHT promoter demonstrated that cholinergic neurons originating from the middle region project to the body wall muscle, gills, oral siphon, and atrial siphon at the juvenile stage 32 .Optogenetic analysis using the channel rhodopsin expressed under the VACHT promoter uncovered that cholinergic neurons derived from the middle part of the ganglion act as motor neurons and are essential for the contraction of the body wall muscle, oral/atrial siphon, and ciliary movement of the gill slit 32 .Furthermore, a pharmacological study using juvenile Ciona demonstrated that acetylcholine is involved in the arrest of the gill cilia 35 .These findings suggest that cholinergic neurons expressing CioR1 also act as motor neurons, and cionin regulates motor neurons through CioR1.In addition, cholinergic neurons also play a pivotal role in the various region of the brain 13 .However, these functions have yet to be elucidated in ascidians.Therefore, distribution and physiological function of CioR1-expressing cholinergic neurons in Ciona await further investigation.
In summary, we clarified the localization of cioninergic neurons in the cerebral ganglion and the presence of CioR1-expressing cholinergic neurons.This study paves the way for investigating the role of neural peptides in the Ciona central nervous system.

Animals
Ciona intestinalis type A (Ciona robusta) was purchased from the National Bio-Resource Project (NBRP) Ciona, which is provided from the Maizuru Fisheries Research Station of Kyoto University or Misaki Marine Biological Station of the University of Tokyo.The ascidians were maintained in the aquarium of the Noto Marine Laboratory.

Whole mount in situ hybridization of Ciona juvenile and adult neural complex
WISH analysis of Ciona juvenile and adult neural complexes was performed as described previously 36 .DIGlabeled RNA probes for cionin and CioR1 were synthesized using a DIG RNA-labeling kit (Roche, Basel, Switzerland).Primer sets for cionin, CioR1, CioR2, and vesicular acetylcholine transporter (VACHT) 37 were designed using NM_001032539, AJ549433, NM_001278980 and KY21.Chr1.783.v1.SL1-1, respectively.The primer sets used for probe synthesis are listed in Table 1.WISH performed by using the sense probes did not show any expression signals (data not shown).www.nature.com/scientificreports/

Immunohistochemistry of the neural complex in adult Ciona
Immunohistochemistry of the adult neural complex was performed as the previous study 18 .Briefly, the neural complex was obtained from an adult individual and fixed overnight in Bouin's solution at room temperature.Ten µm paraffin sections were generated by microtome.After deparaffinization, the sections were incubated with a blocking solution containing 1% normal horse serum and 0.4% Triton X-100 in PBS at room temperature for 1 h.Anti-cionin rabbit antibody (500-fold dilution) in blocking solution was incubated at 4C overnight.The specificity of the antibody was already validated by antibody absorption test 18 .After rinsing with PBS, biotin-conjugated donkey anti-rabbit IgG (1000-fold dilution) was added to the sections and incubated at room temperature for 1 h.After the sections were rinsed with PBS, they were incubated with an avidin-biotinylated HRP complex (ABC, Vector Laboratories, Inc., Burlingame, CA) for 30 min.For color development, the sections were incubated with 0.02% 3,3-diaminobenzidine-tetrachloride and 0.06% hydrogen peroxide in 0.05 M Tris-HCl, pH 7.6) for several minutes.Finally, signals were observed by a BZ-9000 microscope (Keyence, Osaka, Japan).

Double in situ hybridization analysis
Neural complexes were surgically removed from the juvenile specimens fixed in 4% paraformaldehyde.The sections were then dehydrated with ethanol and embedded in polyester wax (BDH; Poole, UK).Embedded neural complexes were sectioned at a thickness of 10 μm.Antisense VACHT RNA probes were synthesized using T7-RNA polymerase (Thermo Fisher Scientific, Pittsburgh, PA, USA) with DIG RNA Labeling Mix (Roche).
Fluorescein RNA Labeled Mix (Roche) was used to synthesize antisense cionin and CioR1 probes using T7-RNA polymerase.The primer sets used for probe synthesis and probe lengths are listed in Table 1.The wax from the neural complex sections was removed using an ethanol series, and the sections were used for in situ hybridization.Two-color in situ hybridization was performed as previously described 38 .First-color staining was performed using the TSA Plus Fluorescein System (PerkinElmer, Waltham, MA, USA) after incubation with anti-fluorescein-HRP (Perkin Elmer).Second-color staining was performed by TSA Plus Cyanine 3 System (PerkinElmer) after incubation with anti-DIG-POD (Roche).The expression signals were observed using an Olympus BX51 microscope (Olympus, Tokyo, Japan).

Figure 1 .Figure 2 .
Figure 1.Immunohistochemical analysis of cionin in serial sections of the Ciona neural complex.(A) Section containing the anterior part of the neural complex, (B) Section containing the anterior and central parts of the neural complex, (C) Section containing the central and posterior parts of the neural complex, (D) Section containing the posterior part of the neural complex.The cg and ng show cerebral ganglion and neural gland, respectively.The a and p describe anterior and posterior, respectively.Scale bars represent 100 µm.

Figure 3 .Figure 4 .
Figure 3. Localization analysis of cionin, CioR1, and VACHT in the adult neural complex.WISH of cionin, CioR1, and VACHT mRNA in the adult neural complex is shown in A, C, and E, respectively.B, D, and F represent sections A, C, and E, respectively.Scale bars in A, C, and E and B, D, and F are 1000 and 200 µm, respectively.